Associated Papers
Unravelling genetic variants of a swedish family with high risk of prostate cancer.
Barilla S et al.
Hereditary Cancer in Clinical Practice, 2022
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
Bmc Medical Genetics, 2020
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Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL1
Breast cancer metastasis to gynaecological organs: a clinico-pathological and molecular profiling study.
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The Journal of Pathology. Clinical Research, 2019
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Supplement: CJP2-5-25-s002.xlsx › SupTable_11__Sequencing_data
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